The graphs represent trends of respiratory parameters in the individual patient at the 3 time points. Before pronation: immediately before initiating noninvasive ventilation (NIV) while the patient was still in the supine position. During pronation: after 1 hour of receiving NIV treatment while the patient was in the prone position. After pronation: 1 hour after NIV treatment stopped when the patient was in the supine position. A, Peripheral oxygen saturation (Spo2), P < .001 between before and during pronation, P < .004 between before and after pronation. B, Arterial partial pressure of oxygen (Pao2) to inspired oxygen fraction (Fio2), P < .001 between before and during pronation, P < .004 between before and after pronation. C, Respiratory rate P < .001 between before and during pronation, P < .001 between before and after pronation.
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Sartini C, Tresoldi M, Scarpellini P, et al. Respiratory Parameters in Patients With COVID-19 After Using Noninvasive Ventilation in the Prone Position Outside the Intensive Care Unit. JAMA. 2020;323(22):2338–2340. doi:10.1001/jama.2020.7861
The pandemic of coronavirus disease 2019 (COVID-19), with a large number of patients requiring respiratory support, threatens to overload intensive care units (ICUs). Noninvasive ventilation (NIV) use in general wards may be an alternative for some patients but has seldom been described and is not used worldwide.1 One study described the feasibility of NIV in the prone position2; pronation can recruit dorsal lung regions and drain airway secretions, improving gas exchange and survival in acute respiratory distress syndrome (ARDS).3 We report respiratory parameters after using this intervention in a case series of patients with COVID-19.
On April 2, 2020, in San Raffaele Scientific Institute, Milan, Italy, COVID-19 patients with ARDS were treated either in the ICUs (n = 48) or medical wards (n = 202). Noninvasive ventilation was used for 62 patients with mild to moderate ARDS who had saturation less than 94% on face mask with high-oxygen concentration, applying 10 cm H2O continuous positive airway pressure and 0.6 fraction of inspired oxygen (Fio2). In case of poor response to NIV, the intensive care physician suggested a trial of NIV in the prone position, which was continued if there was improvement in the first hour of treatment. Noninvasive ventilation cycles were individualized based on a patient’s severity of illness, adherence to the treatment, and dyspnea in the periods without NIV.
On April 2, 2020, we performed a cross-sectional survey to identify all patients undergoing the prone position NIV outside the ICU, irrespective of the day they started using this technique. Respiratory parameters were measured at 3 time points: before NIV, during NIV in pronation (60 minutes after start), and 60 minutes after NIV end. We investigated oxygen saturation as measured by pulse oximetry (Spo2), derived Pao2:Fio2,4 respiratory rate, and patient’s comfort using a numerical rating scale (0, totally uncomfortable, to 10, fully comfortable). Follow-up was conducted at 14 days to determine how many patients were discharged, were still treated in the prone position, or were intubated. Continuous measures were compared using Wilcoxon matched pairs signed rank test or t test if paired data were normally distributed. Two-sided P < .05 defined statistical significance. All analyses were performed with STATA version 16 (STATA Corp). The study was approved by the Ethics Committee of IRCCS San Raffaele Scientific Institute. Written informed consent was obtained.
Fifteen patients receiving NIV in the prone position outside the ICU on April 2 were identified. Mean (SD) age was 59 years (6 years); 13 were men. Noninvasive ventilation in the prone position started a median of 5 days (interquartile range [IQR], 3-10 days) before April 2 (Table) and no patient started NIV in the prone position on April 2. The median number of NIV cycles in the prone position on April 2 was 2 (IQR, 1-3 cycles) for a total duration of 3 hours (IQR, 1-6 hours). Compared with baseline, all patients had a reduction in respiratory rate during and after pronation (P < .001 for both) (Figure); all patients had an improvement in Spo2 and Pao2:Fio2 during pronation (P < .001 for both); 12 patients (80%) had an improvement in Spo2 and Pao2:Fio2 after pronation; 2 (13.3%) had the same value; and 1 (6.7%) had worsened. Compared with baseline, 11 patients (73.3%) had an improvement in comfort during pronation and 4 (26.7%) had the same value; 13 patients (86.7%) had an improvement in comfort after pronation and 2 (13.3%) had the same value. At the 14-day follow-up, 9 patients were discharged home, 1 improved and stopped pronation, 3 continued pronation, 1 patient was intubated and admitted to ICU, and 1 patient died.
Providing NIV in the prone position to patients with COVID-19 and ARDS on the general wards in 1 hospital in Italy was feasible. The respiratory rate was lower and the oxygenation was higher during and after pronation than they were at baseline. Whether intubation was avoided or delayed remains to be determined.
Limitations include the small number of patients, short duration of NIV in the prone position, and lack of a control group. Comparisons of NIV in the prone position with oxygen by face mask or NIV in the standard position are needed. Importantly, selection bias is possible. Patients were not included if NIV failed while in the prone position or were treated and either died or recovered before April 2. Therefore, patients in the study may not be representative of all patients treated with NIV in the prone position.
Correction: This article was corrected online May 26, 2020, to replace the first name with the surname of one of the authors in the Author Contribution section and to identify that it was an intensive care physician who suggested assessing noninvasive ventilation in the prone position.
Corresponding Author: Giovanni Landoni, MD, Vita-Salute San Raffaele University, Department of Anesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60-20132, Milan, Italy (email@example.com).
Accepted for Publication: April 27, 2020.
Published Online: May 15, 2020. doi:10.1001/jama.2020.7861
Author Contributions: Dr Landoni had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: Sartini, Tresoldi, Landoni, Zangrillo.
Acquisition, analysis, or interpretation of data: Sartini, Scarpellini, Tettamanti, Carcò, Landoni.
Drafting of the manuscript: Sartini, Landoni.
Critical revision of the manuscript for important intellectual content: All authors.
Statistical analysis: Sartini.
Administrative, technical, or material support: Sartini, Carcò, Zangrillo.
Supervision: Sartini, Tresoldi, Landoni, Zangrillo.
Additional Contributions: We thank all the medical staff, residents, and nurses of San Raffaele Hospital, especially Francesco Nisi, MD, for careful data collection; Colombo Sergio, MD, and Monti Giacomo, MD, for their support to other colleagues due to clinical expertise in noninvasive ventilation; Silvani Paolo, MD, for his role as coordinator of all the medical emergency teams; Cristallo Edoardo, MD, and Tarzia Valentina, MD, for their first-line help in the management of noninvasive ventilation; and Castelli Elena, DPT, for her contribution in the physical rehabilitation of these patients. None mentioned herein received any compensation for their contribution.
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